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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357283Generated: October 29, 2026

Methanol → 2-[(2,6-Dichloro-3-methylphenyl)amino]benzaldehyde

https://huagongshe.com/reaction/357283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantN-methoxy-N-methyl-2-[(2,6-dichloro-4-methylphenyl)amino]benzamideHCID 18936985—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventTetrahydrofuranHCID 8028—
Product2-[(2,6-Dichloro-3-methylphenyl)amino]benzaldehydeHCID 1502737763%

Reaction Steps

To a magnetically stirred 0° C. solution in dry THF (25 mL) of N-methoxy-N-methyl-2-[(2,6-dichloro-4-methylphenyl)amino]benzamide (3.8 g, 11.2 mmol), prepared as in step 1, was added dropwise diisobutylaluminum hydride (1.0M in THF, 24.6 mL) and the reaction mixture was stirred at ambient temperature for 16 hours. Methanol (5 mL) was added dropwise and the mixture was stirred for 15 minutes until a white precipitate had formed. The reaction mixture was concentrated, the residue was taken up in methanol (10 mL), the insoluble white solid was filtered, and the filtrate was evaporated in vacuo and then purified by chromatography on silica gel (5:1 hexane/CH2Cl2) to provide 2-[(2,6-dichloro-3-methylphenyl)amino]benzaldehyde (1.98 g; 63%) and over reduced alcohol side product (0.70 g; 22%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840758
Source datasetuspto-grants-1998_11
ORD IDord-569e3f0cf38b4282a44e341e8299339e
Source noteuspto-grants-1998_11